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Kiora Pharmaceuticals (7EY) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Kio-104Macular EdemaPhase IIRecruitingSafety, Tolerability and Efficacy of Intravitreal KIO-104 in Patients With Macular EdemaFeb 04, 2025―
100 Μg Kio-301, 50 Μg Kio-301Retinitis PigmentosaPhase IIRecruitingA Phase II Study of Intravitreal KIO-301 in Patients With Late-stage Retinitis PigmentosaOct 03, 2024―
Kio-301Retinitis Pigmentosa, Choroideremiaphase1AndPhase2RecruitingA Phase I/II Dose-escalating Study of the Safety, Tolerability and Efficacy of KIO-301 Administered Intravitreally to Patients With Retinitis Pigmentosa and Choroideremia (ABACUS)Mar 08, 2022―

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases: a. Preclinical testing b. Phase 1 – Safety and dosage c. Phase 2 – Effectiveness and side effects d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Kiora Pharmaceuticals, Inc. (DE:7EY) have in its pipeline
Kiora Pharmaceuticals DE:7EY is currently developing the following drugs: Kio-104, 100 Μg Kio-301, 50 Μg Kio-301, Kio-301. These drug candidates are in various stages of clinical development as the company works toward FDA approval.